NP-MRD: Showing NP-Card for cis-Eutigoside A (NP0086382)

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Record Information

Version

2.0

Created at

2022-04-29 06:41:27 UTC

Updated at

2022-04-29 06:41:27 UTC

NP-MRD ID

NP0086382

Secondary Accession Numbers

None

Natural Product Identification

Common Name

cis-Eutigoside A

Description

[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate belongs to the class of organic compounds known as coumaric acid esters. These are aromatic compounds containing an ester derivative of coumaric acid. cis-Eutigoside A is found in Fragaria x ananassa and Stereospermum acuminatissimum. Based on a literature review very few articles have been published on [(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292208412D          

 32 34  0  0  1  0            999 V2000
   -5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013  -10.3125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868   -9.9000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2868   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -10.3125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -11.1375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579  -11.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -11.5500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -15.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 22 28  1  0  0  0  0
 18 29  1  0  0  0  0
 11 29  1  0  0  0  0
  8 30  2  0  0  0  0
  5 31  1  0  0  0  0
 31 32  2  0  0  0  0
  2 32  1  0  0  0  0
M  END

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
    1.5716    0.9061    1.1767 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5431    0.7713    0.4058 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7513    0.0767    0.8199 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7758   -0.0644    0.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0105   -0.7283    0.3079 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2270   -1.2933    1.5286 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4430   -1.9344    1.7945 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3987   -1.9856    0.8252 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5968   -2.6209    1.0966 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1801   -1.4118   -0.4157 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9948   -0.7829   -0.6854 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4803    1.2856   -0.8617 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4571    1.9673   -1.4762 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1642    1.2113   -1.6755 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3370    0.8390   -0.4777 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6406    0.3073   -0.4912 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0061    0.2870    0.8473 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1747   -0.9231    1.4239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2533   -1.7963    0.9039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6238   -1.2746    1.0324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3294   -0.6115    0.0717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6121   -0.1539    0.3317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2428   -0.3336    1.5428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5294    0.1350    1.7778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5199   -1.0057    2.5056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2479   -1.4652    2.2642 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5834    1.1804   -1.2431 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9598    0.6184   -2.4855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8973    2.5018   -1.6450 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4446    3.0725   -0.4669 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7345    2.0730   -2.5212 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2399    1.3249   -3.5803 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7944   -0.3199    1.8032 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6580    0.3767   -1.0088 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4660   -1.2449    2.2806 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5890   -2.3753    2.7736 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3007   -2.6548    0.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9353   -1.4498   -1.1880 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8062   -0.3304   -1.6455 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2712    2.9071   -0.8633 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8399    2.3825   -2.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4521    0.3328   -2.3298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6176   -0.7173   -0.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2005   -1.4747    1.5375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4497   -0.7181    2.5148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1965   -2.7703    1.4683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1236   -2.0879   -0.1603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8722   -0.4670   -0.8888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1391    0.3651   -0.4481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5851    1.0902    2.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0017   -1.1601    3.4751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6849   -2.0000    3.0443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4964    1.4763   -0.7241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6544    1.2271   -2.8495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6290    3.1234   -2.1889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9008    2.7624    0.3380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1749    2.9550   -2.9023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6042    0.6001   -3.8526 H   0  0  0  0  0  0  0  0  0  0  0  0
 32 31  1  0
 31 14  1  0
 14 13  1  0
 13 12  1  0
 12  2  1  0
  2  1  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 23 25  1  0
 25 26  2  0
 16 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 11  5  1  0
 26 20  1  0
 32 58  1  0
 31 57  1  6
 14 42  1  6
 13 40  1  0
 13 41  1  0
  3 33  1  0
  4 34  1  0
  6 35  1  0
  7 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 16 43  1  6
 18 44  1  0
 18 45  1  0
 19 46  1  0
 19 47  1  0
 21 48  1  0
 22 49  1  0
 24 50  1  0
 25 51  1  0
 26 52  1  0
 27 53  1  1
 28 54  1  0
 29 55  1  6
 30 56  1  0
M  END


  Mrv1652304292208412D          

 32 34  0  0  1  0            999 V2000
   -5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013  -10.3125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868   -9.9000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2868   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -10.3125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -11.1375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8579  -11.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -11.5500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -15.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 22 28  1  0  0  0  0
 18 29  1  0  0  0  0
 11 29  1  0  0  0  0
  8 30  2  0  0  0  0
  5 31  1  0  0  0  0
 31 32  2  0  0  0  0
  2 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0086382

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1[C@@H](COC(=O)C=CC2=CC=C(O)C=C2)O[C@@H](OCCC2=CC=C(O)C=C2)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C23H26O9/c24-16-6-1-14(2-7-16)5-10-19(26)31-13-18-20(27)21(28)22(29)23(32-18)30-12-11-15-3-8-17(25)9-4-15/h1-10,18,20-25,27-29H,11-13H2/t18-,20-,21+,22-,23-/m1/s1

> <INCHI_KEY>
CACGKEKIUJWMQD-DODNOZFWSA-N

> <FORMULA>
C23H26O9

> <MOLECULAR_WEIGHT>
446.452

> <EXACT_MASS>
446.157682417

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
45.338861203527145

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
1.27

> <JCHEM_LOGP>
2.1504816826666655

> <ALOGPS_LOGS>
-3.12

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.26134962540372

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.334668732035519

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6490922422252465

> <JCHEM_POLAR_SURFACE_AREA>
145.91

> <JCHEM_REFRACTIVITY>
113.57169999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.37e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0     -10.669  -7.700   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0     -10.669  -9.240   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.336 -10.010   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -10.669 -12.320   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -10.669 -13.860   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -12.003 -14.630   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -12.003 -16.170   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0     -10.669 -16.940   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0     -10.669 -18.480   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -9.336 -19.250   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -8.002 -18.480   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -8.002 -16.940   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -6.668 -19.250   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -5.335 -18.480   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -6.668 -20.790   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -5.335 -21.560   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -8.002 -21.560   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -8.002 -23.100   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -9.336 -23.870   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -9.336 -25.410   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -8.002 -26.180   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -6.668 -25.410   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.335 -26.180   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.335 -27.720   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -4.001 -28.490   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -6.668 -28.490   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -8.002 -27.720   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -9.336 -20.790   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0     -13.337 -16.940   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0     -12.003 -11.550   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -12.003 -10.010   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   32                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   31                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   30                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   29                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   29                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   22                                                       
CONECT   29   18   11                                                       
CONECT   30    8                                                            
CONECT   31    5   32                                                       
CONECT   32   31    2                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Value	Source
[(2R,3S,4S,5R,6R)-3,4,5-Trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₂₃H₂₆O₉

Average Mass

446.4520 Da

Monoisotopic Mass

446.15768 Da

IUPAC Name

[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate

Traditional Name

[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

O[C@@H]1[C@@H](COC(=O)C=CC2=CC=C(O)C=C2)O[C@@H](OCCC2=CC=C(O)C=C2)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C23H26O9/c24-16-6-1-14(2-7-16)5-10-19(26)31-13-18-20(27)21(28)22(29)23(32-18)30-12-11-15-3-8-17(25)9-4-15/h1-10,18,20-25,27-29H,11-13H2/t18-,20-,21+,22-,23-/m1/s1

InChI Key

CACGKEKIUJWMQD-DODNOZFWSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Fragaria x ananassa	Plant	KNApSAcK
Stereospermum acuminatissimum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumaric acid esters. These are aromatic compounds containing an ester derivative of coumaric acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Coumaric acid esters

Alternative Parents

Substituents

Coumaric acid ester
Cinnamic acid ester
Coumaric acid or derivatives
O-glycosyl compound
Glycosyl compound
Tyrosol derivative
Styrene
1-hydroxy-2-unsubstituted benzenoid
Phenol
Fatty acid ester
Fatty acyl
Benzenoid
Oxane
Monosaccharide
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.27	ALOGPS
logP	2.15	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	9.33	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	145.91 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	113.57 m³·mol⁻¹	ChemAxon
Polarizability	45.34 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162867248

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for cis-Eutigoside A (NP0086382)

MOL for NP0086382 (cis-Eutigoside A)

3D MOL for NP0086382 (cis-Eutigoside A)

3D SDF for NP0086382 (cis-Eutigoside A)

3D-SDF for NP0086382 (cis-Eutigoside A)

PDB for NP0086382 (cis-Eutigoside A)

3D PDB for NP0086382 (cis-Eutigoside A)

SMILES for NP0086382 (cis-Eutigoside A)

INCHI for NP0086382 (cis-Eutigoside A)

Structure for NP0086382 (cis-Eutigoside A)

3D Structure for NP0086382 (cis-Eutigoside A)